Variants with conflicting interpretations "pathogenic" from ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories and "uncertain significance" from any submitter

Minimum review status of the submission from ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories:		Collection method of the submission from ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 13q12.11(chr13:20796981-21104487)x1
GRCh37/hg19 13q31.1(chr13:85812936-86436723)x1
GRCh37/hg19 15q11.2(chr15:22770421-23277435)x1
GRCh37/hg19 15q11.2(chr15:22770421-23282799)x1
GRCh37/hg19 15q11.2(chr15:22770421-23283811)x1
GRCh37/hg19 16p13.11(chr16:14866283-16544419)x3
GRCh37/hg19 17p13.2(chr17:3505567-3557441)x1
GRCh37/hg19 1p35.1(chr1:33490421-33599915)x1
GRCh37/hg19 2q36.3(chr2:228534400-228589902)x1
GRCh37/hg19 9p24.3(chr9:209753-246900)x1

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